I do not know either. I am not discouraged. It will answer many questions, if not, It took 15 year to figure out MP, I never expected MG, but I suspected something was poisoning my nervous system for years.

Today is D-Day and my B-Day. I see the Specialist that wrote the paper on New techniques on diagnosing MG in 2013. At Cleveland Clinic the #2 Research Hospital in the World. I'm sure he will say I do not have MG. Of course as I'm sitting here struggling to breathe, trying to hold my head up, looking blurred vision, 1/2 closed eyes. Been a long road to, this was a surprise diagnosis, I thought I was done and just had to get off my *** and being knocked on my butt every other month was me just not trying hard enough. After a Torn Achallies, MP, Carpal Tunnel (golfers Elbow/MP), CN4 Palsy in the past 8 years.. WTH what is another M.x Disease to add to the pile.